ENST00000261937.11:c.3896G=
MANE Select
|
ENSP00000261937.6:p.Cys1299=
|
|
ENST00000261937.10:c.3896G=
|
ENSP00000261937.6:p.Cys1299=
|
|
ENST00000502603.5:n.596G=
|
|
|
NM_182925.4:c.3896G=
|
NP_891555.2:p.Cys1299=
|
|
XM_011534477.1:c.4145G=
|
XP_011532779.1:p.Cys1382=
|
|
XM_011534478.1:c.4127G=
|
XP_011532780.1:p.Cys1376=
|
|
XM_011534479.1:c.*42G=
|
XP_011532781.1:n.*42G=
|
|
XM_011534482.1:c.3914G=
|
XP_011532784.1:p.Cys1305=
|
|
XM_011534483.1:c.3836G=
|
XP_011532785.1:p.Cys1279=
|
|
XM_011534484.1:c.3437G=
|
XP_011532786.1:p.Cys1146=
|
|
XR_941095.1:n.4182G=
|
|
|
XM_011534478.3:c.4127G=
|
XP_011532780.1:p.Cys1376=
|
|
XM_011534484.2:c.3437G=
|
XP_011532786.1:p.Cys1146=
|
|
XM_017009263.1:c.*42G=
|
XP_016864752.1:n.*42G=
|
|
XM_017009268.1:c.3818G=
|
XP_016864757.1:p.Cys1273=
|
|
XR_001742050.2:n.4386G=
|
|
|
NM_182925.5:c.3896G=
MANE Select
|
NP_891555.2:p.Cys1299=
|
|